Human IL1F7 ELISA Kit

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  • Alternative name

    Interleukin-37 ELISA KIT; FIL1 zeta ELISA KIT; IL-1X ELISA KIT; Interleukin-1 family member 7 ELISA KIT; IL-1F7 ELISA KIT; Interleukin-1 homolog 4 ELISA KIT; IL-1H ELISA KIT; IL-1H4 ELISA KIT; Interleukin-1 zeta ELISA KIT; IL-1 zeta ELISA KIT; Interleukin-1-related protein ELISA KIT; IL-1RP1 ELISA KIT; Interleukin-23 ELISA KIT; IL-37IL37 ELISA KIT; FIL1Z ELISA KIT; IL1F7 ELISA KIT; IL1H4 ELISA KIT; IL1RP1 ELISA KIT; IL-1F7 ELISA KIT; IL-1H ELISA KIT; IL-1H4 ELISA KIT; IL-1 zeta ELISA KIT; IL-1RP1 ELISA KIT; IL-37 ELISA KIT

  • Catalog
    E020425
  • species
    Human
  • GeneIL1F7
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of human IL-37. No significant cross-reactivity or interference between human IL-37 and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of human IL-37 is typically less than 7.81 pg/ml. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined the me
  • Intended UseHuman IL1F7 ELISA Kit allows for the in vitro quantitative determination of IL1F7 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageFor 5-7days:Store the whole kit at 4℃
    For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
  • Product Description
    specifical
    Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for IL-37 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any IL-37 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for IL-37 is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of IL-37 bound in the initial step. The color development is stopped and the intensity of the color is measured.


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